Global Medical Device Quality Systems Requirements

Marketing a medical device in a global environment offers many challenges, as requirements vary widely from one country to another. Bringing a product to market in multiple countries requires understanding those differences and knowing how to comply with all the regulations.

NSF International provides regulatory and quality medical devices training courses and professional qualifications. NSF’s training courses are highly interactive and based on real scenarios, helping you meet international requirements, ensure smooth submissions and keep you ahead of expanding regulatory developments.

From problems with data integrity to properly maintaining complaint files, our training program explains all aspects of the regulations to ensure your product is compliant through all stages of the lifecycle.